GE Medical Systems Information Technologies recall: Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04
GE Medical Systems Information Technologies Inc is recalling Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04 – 29,570 (23,632 US; 5,938 OUS). The U.S. Food and Drug Administration published the recall on September 23, 2026; it began on July 30, 2026. Distributed nationwide.
Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
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| Product | Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04 |
| Brand | GE Medical Systems Information Technologies |
| Company | GE Medical Systems Information Technologies Inc |
| Type | Medical devices |
| Classification | Class II |
| Recall date | July 30, 2026 |
| Published by FDA | September 23, 2026 |
| Quantity | 29,570 (23,632 US; 5,938 OUS) |
| Recall ID | 99637 |
Recalled products
- Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04, 5867474-13 Product code STU CSCS V3 MAI800 Integrated Part Number 5867474-03 Product Code STV
- FDA recall number
- Z-3143-2026
- Codes, lots and dates
- 5867474-04 UDI-DI 00195278343512 Device Serial Numbers begin with STU 5867474-13 UDI-DI 00195278516367 Device Serial Numbers begin with STU 5867474-03 UDI-DI 00195278343383 Device Serial Numbers begin with STV
- Quantity
- 29,570 (23,632 US; 5,938 OUS)
- Classification
- Class II
Identifiers and details
- FDA event ID
- 99637
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Waukesha, WI, United States
Why it was recalled
The reason the FDA lists: “Device may not resume patient monitoring for at least 3 minutes following system restart. Issue can lead to potential delay in recognition of clinically significant events.”
Where it was sold
Nationwide. Distribution as the FDA records it: “Worldwide - US Nationwide distribution.”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99637, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
Other GE Medical Systems Information Technologies recalls
| Date | Recall | Problem | Agency |
|---|---|---|---|
| Sep 2, 2026 |  GE Medical Systems Information Technologies recall: Portrait Core Services Software V1.1 and 3 more productsMedical devices · 23 units; 4 units; 15 units; 0 | Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. I… Serious | FDA Class II |
Other medical device recalls
| Date | Recall | Problem | Agency |
|---|---|---|---|
| Oct 7, 2026 | Draeger recall: VentStar Resus NeoMedical devices · 1,063,643 units | Potential cracks in the hose, which could lead to leakage or the hose falling off. Most serious | FDA Class I |
| Oct 7, 2026 | Medline Industries recall: Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories and 1 more productMedical devices · 771,127 total | a fire hazard Most serious | FDA Class I |
| Oct 7, 2026 | Karl Storz Endoscopy recall: HOPKINS Telescope 30¿Medical devices · 6 eyepieces | Due to incorrect inside packaging label for eyepiece. Serious | FDA Class II |
| Oct 7, 2026 | Noxbox recall: NOxBOXi Nitric Oxide Delivery SystemMedical devices · 1,667 units | Potential for irregular oxygen readings due to a manufacturing issue affecting certain oxy… Serious | FDA Class II |
| Oct 7, 2026 | Siemens Healthcare Diagnostics recall: Atellica CH Revised C-Reactive ProteinMedical devices · 42940 units (3938 US, 39002 OUS) | The potential for falsely elevated results. Serious | FDA Class II |
| Oct 7, 2026 | Tandem Diabetes Care recall: T:slim Mobile ApplicationMedical devices · 177 | A beta (early-release) version of the iOS application, version 2.13 (TestFlight) had a sof… Serious | FDA Class II |
About this recall
Is GE Medical Systems Information Technologies Carescape Central Station CSCS V3 MAS800 Desktop Part Number 5867474-04 recalled?
Yes. GE Medical Systems Information Technologies Inc recalled it on July 30, 2026; FDA published it September 23, 2026 (Class II). Only the lots, dates or models listed on this page are included.
Why was it recalled?
Device may not resume patient monitoring for at least 3 minutes following system restart. Issue can lead to potential delay in recognition of clinically significant events.
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
Nationwide.
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.